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Non-adherent intervention for Colorectal Cancer

N/A
Waitlist Available
Research Sponsored by University of Rochester
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 150 days
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a program that sends motivational text messages to patients who are not getting recommended colorectal cancer screenings. The messages aim to encourage these patients to get screened. The goal is to see if these reminders help more people follow through with their screenings.

Eligible Conditions
  • Colorectal Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~150 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 150 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Screening
Secondary study objectives
Phone Interview for refinement of Intervention

Side effects data

From 2019 Phase 4 trial • 136 Patients • NCT02584140
45%
Decreased Creatinine Clearance
4%
Abdominal Discomfort
3%
Headache
100%
80%
60%
40%
20%
0%
Study treatment Arm
AEGIS

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Non-adherent interventionExperimental Treatment1 Intervention
Intervention subjects will receive the text messaging intervention and a 150 day follow-up phone call.
Group II: Non-adherent controlActive Control1 Intervention
Control subjects will receive no text intervention and a 150 day follow-up phone call.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Text Messaging
2016
Completed Phase 4
~3970

Find a Location

Who is running the clinical trial?

University of RochesterLead Sponsor
866 Previous Clinical Trials
545,262 Total Patients Enrolled
~31 spots leftby Nov 2025
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